BEUDAMED
    36 results · 34ms · Sources: EU EUDAMED, US FDA

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    MEDTRONIC DLP ARTERIAL CANNULAE WITH 3D TIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741142611·Catheter Placement Kit

    TEWA

    FDA UDI
    asia-med GmbH·04251282513818·TeWa JJ-Type 2225: coated acupuncture needles ...

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282506803·TeWa JJ-Type 2225: coated acupuncture needles ...

    CoAxia FloControl™ Catheter

    FDA UDI
    Zoll Circulation, Inc.·00849111030014·The CoAxia FloControl™ Catheter is a 7F multi-l...

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·June 5, 2024

    CELL-CHEX

    FDA 510(k)
    FDA Class 2 ·Hematology

    MPT 24 AND VITAL VIEW 24

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 26, 2024

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·September 23, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·July 10, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·February 20, 2025

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 12, 2013

    TRAJECTORY GUIDE KIT, BIOPSY, EXTERNAL

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC.·Product code HAW·February 17, 2011

    NX3

    FDA Adverse Event
    Malfunction ·KERR CORPORATION·Product code EMA·February 21, 2008